| Organism name | Pterocaulon alopecuroides |
|---|---|
| Genus | Pterocaulon |
| Family | Asteraceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Pterocaulon |
|---|---|
| Linked NCBI taxonomy ID | 81513 |
| Linked level | genus |
| Family in NCBI taxonomy | Asteraceae |
|---|---|
| ID | 4210 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | asterids |
|---|---|
| ID | 71274 |
| KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
KCF-S
cluster |
phytochemical
cluster |
figure |
|---|---|---|---|---|---|---|---|---|
|
C00008636
|
7-O-Prenyltaxifolin
|
No. 276 | No. 14 |
|
||||
|
C00019845
|
7-(2,3-Dihydroxy-3-methylbutyloxy)-5-hydroxy-5-methoxycoumarin
|
CHEMBL1574904
|
8 / 9 / 7 | No. 579 | No. 25 |
|
||
|
C00019846
|
7-(2,3-Dihydroxy-3-methylbutyloxy)-5-hydroxy-6-methoxycoumarin
|
No. 579 | No. 25 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P06746 | DNA polymerase beta | Enzyme | C00019845 | 0 / 0 |
| P04062 | Glucosylceramidase | Enzyme | C00019845 | 6 / 4 |
| P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00019845 | 2 / 2 |
| P06280 | Alpha-galactosidase A | Enzyme | C00019845 | 1 / 1 |
| Q9UNA4 | DNA polymerase iota | Enzyme | C00019845 | 0 / 0 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00019845 | 0 / 0 |
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00019845 | 0 / 0 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00019845 | 0 / 0 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #301500 | Fabry disease |
P06280
|
| #608013 | Gaucher disease, perinatal lethal |
P04062
|
| #230800 | Gaucher disease, type i |
P04062
|
| #230900 | Gaucher disease, type ii |
P04062
|
| #231000 | Gaucher disease, type iii |
P04062
|
| #231005 | Gaucher disease, type iiic |
P04062
|
| #257200 | Niemann-pick disease, type a |
P17405
|
| #607616 | Niemann-pick disease, type b |
P17405
|
| #168600 | Parkinson disease, late-onset; pd |
P04062
|
| KEGG | name | UniProt |
|---|---|---|
| H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
| H00126 | Gaucher disease |
P04062
(related)
|
| H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
| H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
| H00125 | Fabry disease |
P06280
(related)
|
| H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
| H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|